Aboul-Enein H Y, Serignese V
Bioanalytical and Drug Development Laboratory, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Biomed Chromatogr. 1997 Jan-Feb;11(1):47-9. doi: 10.1002/(SICI)1099-0801(199701)11:1<47::AID-BMC626>3.0.CO;2-M.
A direct, isocratic high-performance liquid chromatographic (HPLC) method is described for the enantiomeric separation of racemic cathinone and one of its metabolites (+/-)-norephedrine, on a protein-based chiral stationary phase (CSP), cellobiohydrolase, known as CBH-I, under reversed-phase conditions. It was determined that the S-(-)-enantiomer eluted first for cathinone while the 1S,2R-(+)-enantiomer eluted first for norephedrine. The procedure is simple with no sample derivatization required and a short assay time.